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Functional analysis of RF2a, a rice transcription factor.

Authors :
Dai S
Petruccelli S
Ordiz MI
Zhang Z
Chen S
Beachy RN
Source :
The Journal of biological chemistry [J Biol Chem] 2003 Sep 19; Vol. 278 (38), pp. 36396-402. Date of Electronic Publication: 2003 Jul 10.
Publication Year :
2003

Abstract

RF2a is a bZIP transcription factor that regulates expression of the promoter of rice tungro bacilliform badnavirus. RF2a is predicted to include three domains that contribute to its function. The results of transient assays with mutants of RF2a from which one or more domains were removed demonstrated that the acidic domain was essential for the activation of gene expression, although the proline-rich and glutamine-rich domains each played a role in this function. Studies using fusion proteins of different functional domains of RF2a with the 2C7 synthetic zinc finger DNA-binding domain showed that the acidic region is a relatively strong activation domain, the function of which is dependent on the context in which the domain is placed. Data from transgenic plants further supported the conclusion that the acidic domain was important for maintaining the biological function of RF2a. RF2a and TBP (TATA-binding protein) synergistically activate transcription in vitro (Zhu, Q., Ordiz, M. I., Dabi, T., Beachy, R. N., and Lamb, C. (2002) Plant Cell 14, 795-803). In vitro and in vivo assays showed that RF2a interacts with TBP through the glutamine-rich domain but not the acidic domain. Functional analysis of such interactions indicates that the acidic domain activates transcription through mechanisms other than via the direct recruitment of TBP.

Details

Language :
English
ISSN :
0021-9258
Volume :
278
Issue :
38
Database :
MEDLINE
Journal :
The Journal of biological chemistry
Publication Type :
Academic Journal
Accession number :
12855676
Full Text :
https://doi.org/10.1074/jbc.M304862200